These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

243 related articles for article (PubMed ID: 30003711)

  • 81. Fetal phenotype of Prader-Willi syndrome due to maternal disomy for chromosome 15.
    L'Herminé AC; Aboura A; Brisset S; Cuisset L; Castaigne V; Labrune P; Frydman R; Tachdjian G
    Prenat Diagn; 2003 Nov; 23(11):938-43. PubMed ID: 14634983
    [TBL] [Abstract][Full Text] [Related]  

  • 82. Maternal uniparental disomy in a patient with Prader-Willi syndrome with an additional small inv dup(15) chromosome.
    Wang YM; Chuang L; Wang BT; Kuo PL
    J Formos Med Assoc; 2004 Dec; 103(12):943-7. PubMed ID: 15624046
    [TBL] [Abstract][Full Text] [Related]  

  • 83. Imprinting center analysis in Prader-Willi and Angelman syndrome patients with typical and atypical phenotypes.
    Camprubí C; Coll MD; Villatoro S; Gabau E; Kamli A; Martínez MJ; Poyatos D; Guitart M
    Eur J Med Genet; 2007; 50(1):11-20. PubMed ID: 17095305
    [TBL] [Abstract][Full Text] [Related]  

  • 84. Zinc finger protein 274 regulates imprinted expression of transcripts in Prader-Willi syndrome neurons.
    Langouët M; Glatt-Deeley HR; Chung MS; Dupont-Thibert CM; Mathieux E; Banda EC; Stoddard CE; Crandall L; Lalande M
    Hum Mol Genet; 2018 Feb; 27(3):505-515. PubMed ID: 29228278
    [TBL] [Abstract][Full Text] [Related]  

  • 85. De novo interstitial duplication of 15q11.2-q13.1 with complex maternal uniparental trisomy for the 15q11-q13 region in a patient with Prader-Willi syndrome.
    Burrage LC; Person RE; Flores A; Villanos MT; Bi W; Wiszniewska J; Bacino CA
    Am J Med Genet A; 2012 Oct; 158A(10):2557-63. PubMed ID: 22903639
    [TBL] [Abstract][Full Text] [Related]  

  • 86. Diagnosis of the Prader-Willi syndrome by proving the absence of the unmethylated PW71 DNA fragment.
    Lindgren AC; Grandell U; Ritzén EM; Anvret M
    Acta Paediatr; 1996 Feb; 85(2):195-8. PubMed ID: 8640049
    [TBL] [Abstract][Full Text] [Related]  

  • 87. Routine screening for microdeletions by FISH in 77 patients suspected of having Prader-Willi or Angelman syndromes using YAC clone 273A2 (D15S10).
    Erdel M; Schuffenhauer S; Buchholz B; Barth-Witte U; Köchl S; Utermann B; Duba HC; Utermann G
    Hum Genet; 1996 Jun; 97(6):784-93. PubMed ID: 8641697
    [TBL] [Abstract][Full Text] [Related]  

  • 88. Comprehensive methylation analysis in typical and atypical PWS and AS patients with normal biparental chromosomes 15.
    Runte M; Färber C; Lich C; Zeschnigk M; Buchholz T; Smith A; Van Maldergem L; Bürger J; Muscatelli F; Gillessen-Kaesbach G; Horsthemke B; Buiting K
    Eur J Hum Genet; 2001 Jul; 9(7):519-26. PubMed ID: 11464243
    [TBL] [Abstract][Full Text] [Related]  

  • 89. Brain-stem serotonin transporter availability in maternal uniparental disomy and deletion Prader-Willi syndrome.
    Krishnadas R; Cooper SA; Nicol A; Pimlott S; Soni S; Holland AJ; McArthur L; Cavanagh J
    Br J Psychiatry; 2018 Jan; 212(1):57-58. PubMed ID: 29433608
    [TBL] [Abstract][Full Text] [Related]  

  • 90. A Comprehensive Review of Genetically Engineered Mouse Models for Prader-Willi Syndrome Research.
    Kummerfeld DM; Raabe CA; Brosius J; Mo D; Skryabin BV; Rozhdestvensky TS
    Int J Mol Sci; 2021 Mar; 22(7):. PubMed ID: 33807162
    [TBL] [Abstract][Full Text] [Related]  

  • 91. Transmission of a Novel Imprinting Center Deletion Associated With Prader-Willi Syndrome Through Three Generations of a Chinese Family: Case Presentation, Differential Diagnosis, and a Lesson Worth Thinking About.
    Zhang K; Liu S; Gu W; Lv Y; Yu H; Gao M; Wang D; Zhao J; Li X; Gai Z; Zhao S; Liu Y; Yuan Y
    Front Genet; 2021; 12():630650. PubMed ID: 34504512
    [TBL] [Abstract][Full Text] [Related]  

  • 92. DNA methylation analysis with respect to prenatal diagnosis of the Angelman and Prader-Willi syndromes and imprinting.
    Glenn CC; Deng G; Michaelis RC; Tarleton J; Phelan MC; Surh L; Yang TP; Driscoll DJ
    Prenat Diagn; 2000 Apr; 20(4):300-6. PubMed ID: 10740202
    [TBL] [Abstract][Full Text] [Related]  

  • 93. A modified MS-PCR approach to diagnose patients with Prader-Willi and Angelman syndrome.
    Dos Santos JF; Mota LR; Rocha PH; Ferreira de Lima RL
    Mol Biol Rep; 2016 Nov; 43(11):1221-1225. PubMed ID: 27535666
    [TBL] [Abstract][Full Text] [Related]  

  • 94. Clinical-etiologic correlation in children with Prader-Willi syndrome (PWS): an interdisciplinary study.
    Torrado M; Araoz V; Baialardo E; Abraldes K; Mazza C; Krochik G; Ozuna B; Leske V; Caino S; Fano V; Chertkoff L
    Am J Med Genet A; 2007 Mar; 143A(5):460-8. PubMed ID: 17163531
    [TBL] [Abstract][Full Text] [Related]  

  • 95. The genetic basis for Prader-Willi syndrome: the importance of imprinted genes.
    Brøndum-Nielsen K
    Acta Paediatr Suppl; 1997 Nov; 423():55-7. PubMed ID: 9401540
    [TBL] [Abstract][Full Text] [Related]  

  • 96. A nonimprinted Prader-Willi Syndrome (PWS)-region gene regulates a different chromosomal domain in trans but the imprinted pws loci do not alter genome-wide mRNA levels.
    Stefan M; Portis T; Longnecker R; Nicholls RD
    Genomics; 2005 May; 85(5):630-40. PubMed ID: 15820315
    [TBL] [Abstract][Full Text] [Related]  

  • 97. Unique maternal deletion of 15q in a patient with some symptoms of Prader-Willi syndrome.
    Ninomiya S; Yokoyama Y; Kawakami M; Une T; Maruyama H; Morishima T
    Pediatr Int; 2005 Oct; 47(5):541-5. PubMed ID: 16190961
    [TBL] [Abstract][Full Text] [Related]  

  • 98. Analysis of parent of origin specific DNA methylation at SNRPN and PW71 in tissues: implication for prenatal diagnosis.
    Kubota T; Aradhya S; Macha M; Smith AC; Surh LC; Satish J; Verp MS; Nee HL; Johnson A; Christan SL; Ledbetter DH
    J Med Genet; 1996 Dec; 33(12):1011-4. PubMed ID: 9004133
    [TBL] [Abstract][Full Text] [Related]  

  • 99. Clinical Application of an Innovative Multiplex-Fluorescent-Labeled STRs Assay for Prader-Willi Syndrome and Angelman Syndrome.
    Zhang K; Liu S; Feng B; Yang Y; Zhang H; Dong R; Liu Y; Gai Z
    PLoS One; 2016; 11(2):e0147824. PubMed ID: 26841067
    [TBL] [Abstract][Full Text] [Related]  

  • 100. Prader-Willi syndrome.
    Cassidy SB; Driscoll DJ
    Eur J Hum Genet; 2009 Jan; 17(1):3-13. PubMed ID: 18781185
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 13.